chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	122004188	122004189	C	G	38	GENIC	homozygous	116689764
8	122029518	122029518		ATA	9	GENIC	homozygous	128640217
8	122029479	122029483	CACT		8	GENIC	heterozygous	128640214
8	122029495	122029495		CTC	9	GENIC	heterozygous	128640215
8	122029496	122029497	A		9	GENIC	heterozygous	128640216
8	122029519	122029520	C		10	GENIC	homozygous	128640218
8	122039897	122039898	A	T	43	GENIC	homozygous	116689766
8	122055397	122055398	G	A	15	GENIC	homozygous	116689768
8	122053371	122053372	A	C	35	GENIC	homozygous	116988349
8	122056046	122056047	G	A	54	GENIC	homozygous	116689770
8	122056147	122056148	T		47	GENIC	homozygous	128640219
8	122057046	122057047	A	G	32	GENIC	heterozygous	116689776
8	122062631	122062631		CTTTTTTCC	51	GENIC	homozygous	128640222
8	122066522	122066594	TTCCTGGGATTGAGAGTTCTTTTTTTTTTTTTAAGATTTATTCATTTATTATATATAAGTACACTGCAGCTG		15	GENIC	heterozygous	128640223
8	122068148	122068149	T		50	GENIC	homozygous	128640225
8	122095745	122095746	C	G	15	GENIC	heterozygous	117149838
8	122126673	122126674	C	T	50	GENIC	homozygous	116689778
8	122174255	122174256	G	C	42	GENIC	homozygous	116689784
8	122132577	122132578	G	T	60	GENIC	heterozygous	131061633
8	122132587	122132588	G	T	60	GENIC	heterozygous	131061634
8	122132589	122132590	A	G	58	GENIC	heterozygous	131061635
8	122180542	122180543	C	T	40	GENIC	homozygous	116689786